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D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol

Base Information
  • Chemical Name:D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol
  • CAS No.:200272-93-1
  • Molecular Formula:C26H30O6
  • Molecular Weight:438.521
  • Hs Code.:
D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol

Synonyms:

Suppliers and Price of D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol
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Chemical Property of D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol
Chemical Property:
Purity/Quality:
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Technology Process of D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol

There total 12 articles about D-6-O-benzyl-3-O-benzoyl-1,2-O-cyclohexylidene-4-deoxy-neoinositol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 7 steps
1: 90 percent / H2SO4 / dimethylformamide / 12 h / Ambient temperature
2: 90 percent / triphenylphosphine, carbon tetrachloride, pyridine / 8 h / 60 °C
3: 1.) potassium hydroxide, benzyltrimethylammonium chloride / 1.) CH2Cl2, 10 min, 2.) CH2Cl2, 12 h
4: 60 percent / sodium hydride / dimethylformamide / 3 h / 110 °C
5: 1.) HgCl2, 2.) thiourea / 1.) acetone-d6, D2O, 20 min, 2.) acetone-d6, D2O
6: 30 percent / lithium tri-terbutoxyaluminiumhydride / tetrahydrofuran / -40 °C / other reagent: cerium(III) chloride heptahydrate, sodium borohydride
7: pyridine / 2 h
With pyridine; tetrachloromethane; potassium hydroxide; sulfuric acid; benzyltrimethylammonium chloride; sodium hydride; lithium tri-t-butoxyaluminum hydride; thiourea; triphenylphosphine; mercury dichloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(97)10101-6
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) potassium hydroxide, benzyltrimethylammonium chloride / 1.) CH2Cl2, 10 min, 2.) CH2Cl2, 12 h
2: 60 percent / sodium hydride / dimethylformamide / 3 h / 110 °C
3: 1.) HgCl2, 2.) thiourea / 1.) acetone-d6, D2O, 20 min, 2.) acetone-d6, D2O
4: 30 percent / lithium tri-terbutoxyaluminiumhydride / tetrahydrofuran / -40 °C / other reagent: cerium(III) chloride heptahydrate, sodium borohydride
5: pyridine / 2 h
With pyridine; potassium hydroxide; benzyltrimethylammonium chloride; sodium hydride; lithium tri-t-butoxyaluminum hydride; thiourea; mercury dichloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(97)10101-6
Guidance literature:
Multi-step reaction with 6 steps
1: 90 percent / triphenylphosphine, carbon tetrachloride, pyridine / 8 h / 60 °C
2: 1.) potassium hydroxide, benzyltrimethylammonium chloride / 1.) CH2Cl2, 10 min, 2.) CH2Cl2, 12 h
3: 60 percent / sodium hydride / dimethylformamide / 3 h / 110 °C
4: 1.) HgCl2, 2.) thiourea / 1.) acetone-d6, D2O, 20 min, 2.) acetone-d6, D2O
5: 30 percent / lithium tri-terbutoxyaluminiumhydride / tetrahydrofuran / -40 °C / other reagent: cerium(III) chloride heptahydrate, sodium borohydride
6: pyridine / 2 h
With pyridine; tetrachloromethane; potassium hydroxide; benzyltrimethylammonium chloride; sodium hydride; lithium tri-t-butoxyaluminum hydride; thiourea; triphenylphosphine; mercury dichloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(97)10101-6
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